Evidence map›Paper›PMID 42045613›Full record

ArticleJournal of community genetics2026

Family quality of life in the context of Rett syndrome: insights from Brazilian families.

Nicoly Stefani Sevalho Carlucci, Bianca Pereira Favilla, Beatriz Carvalho Nunes, Fernanda Teresa de Lima, Maria Isabel Melaragno, Rui Fernando Pilotto, Lucimar Retto da Silva de Avó, Carla Maria Ramos Germano, Débora Gusmão Melo

Abstract read
In one paragraph

Article in Journal of community genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Nicoly Stefani Sevalho CarlucciDepartment of Medicine, Universidade Federal de São Carlos (UFSCar), São Paulo, São Carlos, Brazil.ORCID http://orcid.org/0000-0002-6900-7441
Bianca Pereira FavillaGenetics Division, Department of Morphology and Genetics, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-3988-7708
Beatriz Carvalho NunesGenetics Division, Department of Morphology and Genetics, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-1230-1113
Fernanda Teresa de LimaDepartment of Gynecology, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-9266-9964
Maria Isabel MelaragnoGenetics Division, Department of Morphology and Genetics, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-4344-9698
Rui Fernando PilottoDepartment of Genetics, Universidade Federal do Paraná (UFPR), Curitiba, Paraná, Brazil.ORCID http://orcid.org/0000-0001-6835-8138
Lucimar Retto da Silva de AvóDepartment of Medicine, Universidade Federal de São Carlos (UFSCar), São Paulo, São Carlos, Brazil.ORCID http://orcid.org/0000-0001-7282-420X
Carla Maria Ramos GermanoDepartment of Medicine, Universidade Federal de São Carlos (UFSCar), São Paulo, São Carlos, Brazil.ORCID http://orcid.org/0000-0001-5030-7164
Débora Gusmão MeloGenetics Division, Department of Morphology and Genetics, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, São Paulo, Brazil. dgmelo@unifesp.br.ORCID http://orcid.org/0000-0001-7005-3544

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rett syndrome (RTT) is a rare genetic neurodevelopmental disorder characterized by intellectual disability and severe functional impairments, placing a significant burden on affected families. This exploratory cross-sectional study evaluated family quality of life (FQoL) in Brazilian families of girls with RTT and examined its relationship with sociodemographic and clinical variables. Seventy Brazilian families participated in the study. Data were collected using sociodemographic and clinical questionnaires, the Pediatric Quality of Life Inventory, and the Beach Center Family Quality of Life Scale, which assesses five domains: family interaction, parenting, emotional well-being, physical and material well-being, and disability-related support. The average FQoL score was 3.68 ± 0.67, below the satisfaction threshold (4.0). Emotional well-being had the lowest score (3.16 ± 0.96), significantly lower than other domains (p < 0.001). Overall FQoL was associated with factors such as family income, access to welfare benefits and private health insurance, parental education and employment status, as well as individual characteristics of the person with RTT, including age, aggressiveness, and school type. Taken together, aggressiveness, attendance at a regular school, and a monthly income exceeding four official Brazilian minimum wages explained 29.8% of the variance in FQoL scores. The findings underscore the multifactorial nature of FQoL in the context of developmental disabilities. Improving FQoL for families of individuals with RTT requires integrated strategies that combine emotional support for caregivers, socioeconomic assistance, inclusive education, and medical and psychological care for individuals with RTT. These approaches have direct implications for public policies and service provision in low- and middle-income countries.

Indexed as

BrazilFamilyIntellectual disabilityQuality of lifeRare diseasesRett syndromeSocioeconomic factors

Identifiers

PMID42045613
PMCPMC13121640

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.